2. Academic Validation
  3. ZHX2 emerges as a negative regulator of mitochondrial oxidative phosphorylation during acute liver injury

ZHX2 emerges as a negative regulator of mitochondrial oxidative phosphorylation during acute liver injury

  • Nat Commun. 2023 Nov 18;14(1):7527. doi: 10.1038/s41467-023-43439-0.
Yankun Zhang 1,  Yuchen Fan 2,  Huili Hu 3,  Xiaohui Zhang 3,  Zehua Wang 1,  Zhuanchang Wu 1,  Liyuan Wang 1,  Xiangguo Yu 1,  Xiaojia Song 1,  Peng Xiang 1,  Xiaodong Zhang 1,  Tixiao Wang 1,  Siyu Tan 1,  Chunyang Li 1 4,  Lifen Gao 1,  Xiaohong Liang 1,  Shuijie Li 5,  Nailin Li 6,  Xuetian Yue 7 8,  Chunhong Ma 9
Affiliations

Affiliations

  • 1 Key Laboratory for Experimental Teratology of Ministry of Education, School of Basic Medical Sciences, Qilu Hospital, Cheeloo Medical College of Shandong University, Jinan, China.
  • 2 Department of Hepatology, Qilu Hospital of Shandong University, Jinan, China.
  • 3 Institute of Molecular Medicine and Genetics, School of Basic Medical Sciences, Shandong University, Jinan, China.
  • 4 Department of Histology and Embryology, School of Basic Medical Sciences, Shandong University, Jinan, China.
  • 5 College of Pharmacy, Harbin Medical University, Harbin, China.
  • 6 Department of Medicine-Solna, Cardiovascular Medicine Unit, Karolinska Institute, Stockholm, Sweden.
  • 7 Key Laboratory for Experimental Teratology of Ministry of Education, School of Basic Medical Sciences, Qilu Hospital, Cheeloo Medical College of Shandong University, Jinan, China. yuexu@sdu.edu.cn.
  • 8 Department of Cell Biology, School of Basic Medical Sciences, Cheeloo College of Medicine, Shandong University, Jinan, China. yuexu@sdu.edu.cn.
  • 9 Key Laboratory for Experimental Teratology of Ministry of Education, School of Basic Medical Sciences, Qilu Hospital, Cheeloo Medical College of Shandong University, Jinan, China. machunhong@sdu.edu.cn.
PMID: 37980429 DOI: 10.1038/s41467-023-43439-0
Abstract

Mitochondria dysfunction contributes to acute liver injuries, and mitochondrial regulators, such as PGC-1α and MCJ, affect liver regeneration. Therefore, identification of mitochondrial modulators may pave the way for developing therapeutic strategies. Here, ZHX2 is identified as a mitochondrial regulator during acute liver injury. ZHX2 both transcriptionally inhibits expression of several mitochondrial electron transport chain genes and decreases PGC-1α stability, leading to reduction of mitochondrial mass and OXPHOS. Loss of Zhx2 promotes liver recovery by increasing mitochondrial OXPHOS in mice with partial hepatectomy or CCl4-induced liver injury, and inhibition of PGC-1α or electron transport chain abolishes these effects. Notably, ZHX2 expression is higher in liver tissues from patients with drug-induced liver injury and is negatively correlated with mitochondrial mass marker TOM20. Delivery of shRNA targeting Zhx2 effectively protects mice from CCl4-induced liver injury. Together, our data clarify ZHX2 as a negative regulator of mitochondrial OXPHOS and a potential target for developing strategies for improving liver recovery after acute injuries.

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